Leksands Knackebrod AB
FDA import alert and refusal historyLeksand, SwedenFEI 3006335077
As of October 26, 2026, Leksands Knackebrod AB has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 28, 2019, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Leksands Knackebrod AB
2 records, newest first. Each line links to the FDA page it came from.
Questions about Leksands Knackebrod AB
- Is Leksands Knackebrod AB on an FDA import alert?
- No listing for Leksands Knackebrod AB appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Sweden page.
- Has FDA refused shipments from Leksands Knackebrod AB?
- No FDA import refusals for Leksands Knackebrod AB appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Leksands Knackebrod AB last inspected by FDA?
- FDA's most recent inspection of Leksands Knackebrod AB with a final classification is dated August 28, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Leksands Knackebrod AB's FEI number?
- Leksands Knackebrod AB's FDA Establishment Identifier (FEI) is 3006335077.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.